Literature DB >> 24724984

Successful hematopoietic stem cell transplantation in a patient with congenital dyserythropoietic anemia type II.

Sule Unal1, Roberta Russo, Fatma Gumruk, Baris Kuskonmaz, Mualla Cetin, Tulin Sayli, Betul Tavil, Concetta Langella, Achille Iolascon, Duygu Uckan Cetinkaya.   

Abstract

CDA are a group of inherited, rare diseases that are characterized by dyserythropoiesis and ineffective erythropoiesis associated with transfusion dependency in approximately 10% of cases. For these latter patients, the only curative treatment is HSCT. There are very limited data on HSCT experience in this rare disease. Herein, we report a five-yr six-month-old girl with compound heterozygous mutations in SEC23B gene, who was diagnosed to have CDA type II and underwent successful HSCT from her matched sibling donor.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  SEC23B; congenital dyserythropoietic anemias; iron; transplantation

Mesh:

Substances:

Year:  2014        PMID: 24724984     DOI: 10.1111/petr.12254

Source DB:  PubMed          Journal:  Pediatr Transplant        ISSN: 1397-3142


  7 in total

1.  Non-myeloablative allogeneic stem cell transplant with post-transplant cyclophosphamide cures the first adult patient with congenital dyserythropoietic anemia.

Authors:  A Oh; P R Patel; N Aardsma; S R Mehendale; R Chowdhery; K Sweiss; D Rondelli
Journal:  Bone Marrow Transplant       Date:  2017-03-20       Impact factor: 5.483

2.  Stem cell transplantation for congenital dyserythropoietic anemia: an analysis from the European Society for Blood and Marrow Transplantation.

Authors:  Maurizio Miano; Dirk-Jan Eikema; Mahmoud Aljurf; Pieter J Van't Veer; Gülyüz Öztürk; Matthias Wölfl; Frans Smiers; Angsar Schulz; Gerard Socié; Kim Vettenranta; Cristina Diaz de Heredia; Marco Zecca; Johan Maertens; Montserrat Rovira; Jorge Sierra; Duygu Uckan-Cetinkaya; Elena Skorobogatova; Ali Bülent Antmen; Jean-Hugues Dalle; Miroslaw Markiewicz; Rose Marie Hamladji; Vassiliki Kitra-Roussou; Giorgio La Nasa; Gergely Kriván; Amal Al-Seiraihy; Stefano Giardino; Antonio Maria Risitano; Regis Peffault de Latour; Carlo Dufour
Journal:  Haematologica       Date:  2019-01-24       Impact factor: 9.941

Review 3.  The congenital dyserythropoieitic anemias: genetics and pathophysiology.

Authors:  Richard King; Patrick J Gallagher; Rami Khoriaty
Journal:  Curr Opin Hematol       Date:  2021-12-24       Impact factor: 3.218

4.  CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia.

Authors:  Cristian Tornador; Edgar Sánchez-Prados; Beatriz Cadenas; Roberta Russo; Veronica Venturi; Immacolata Andolfo; Ines Hernández-Rodriguez; Achille Iolascon; Mayka Sánchez
Journal:  Front Physiol       Date:  2019-09-13       Impact factor: 4.566

5.  SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.

Authors:  Barbara Eleni Rosato; Roberta Marra; Vanessa D'Onofrio; Federica Del Giudice; Simone Della Monica; Achille Iolascon; Immacolata Andolfo; Roberta Russo
Journal:  Int J Mol Sci       Date:  2022-01-24       Impact factor: 5.923

6.  Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene.

Authors:  Fatih Demircioğlu; Mustafa Erkoçoğlu; Mustafa Dilek; Mervan Bekdaş; Sevil Göksügür; Semra Büyükkorkmaz; Seher Açar
Journal:  Turk J Haematol       Date:  2015-09       Impact factor: 1.831

7.  RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.

Authors:  Gianluca De Rosa; Immacolata Andolfo; Roberta Marra; Francesco Manna; Barbara Eleni Rosato; Achille Iolascon; Roberta Russo
Journal:  Int J Mol Sci       Date:  2020-08-04       Impact factor: 5.923

  7 in total

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